Hasil Pencarian - Ryo Inuzuka
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A novel pathogenic variant located just upstream of the C‐terminal Ser423‐X‐Ser425 phosphorylation motif in SMAD3 causing Loeys–Dietz syndrome oleh Satoshi Ishii, Takayuki Fujiwara, Hiroki Yagi, Norifumi Takeda, Masahiko Ando, Haruo Yamauchi, Ryo Inuzuka, Yuki Taniguchi, Masaru Hatano, Issei Komuro
Diterbitkan 2023-12-01Dapatkan teks lengkap
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Noonan syndrome‐associated biallelic LZTR1 mutations cause cardiac hypertrophy and vascular malformations in zebrafish oleh Yu Nakagama, Norihiko Takeda, Seishi Ogawa, Hiroyuki Takeda, Yoshiyuki Furutani, Toshio Nakanishi, Tatsuyuki Sato, Yoichiro Hirata, Akira Oka, Ryo Inuzuka
Diterbitkan 2020-03-01Dapatkan teks lengkap
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Family with congenital contractural arachnodactyly due to a novel multiexon deletion of the FBN2 gene oleh Hiroki Yagi, Hiroshi Takiguchi, Norifumi Takeda, Ryo Inuzuka, Yuki Taniguchi, Kristine Joyce Porto, Hiroyuki Ishiura, Jun Mitsui, Hiroyuki Morita, Issei Komuro
Diterbitkan 2022-02-01Dapatkan teks lengkap
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Association Between Maternal Factors in Early Pregnancy and Congenital Heart Defects in Offspring: The Japan Environment and Children's Study oleh Shun Kawai, Kyongsun Pak, Shintaro Iwamoto, Chihiro Kawakami, Ryo Inuzuka, Jun Maeda, Yoshiyuki Furutani, Mitsuhiro Kamisago, Shunichi Takatsuki, Tomomi Uyeda, Hiroyuki Yamagishi, Shuichi Ito, Tohru Kobayashi
Diterbitkan 2023-09-01Dapatkan teks lengkap
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Macrophage hypoxia signaling regulates cardiac fibrosis via Oncostatin M oleh Hajime Abe, Norihiko Takeda, Takayuki Isagawa, Hiroaki Semba, Satoshi Nishimura, Masaki Suimye Morioka, Yu Nakagama, Tatsuyuki Sato, Katsura Soma, Katsuhiro Koyama, Masaki Wake, Manami Katoh, Masataka Asagiri, Michael L. Neugent, Jung-whan Kim, Christian Stockmann, Tomo Yonezawa, Ryo Inuzuka, Yasushi Hirota, Koji Maemura, Takeshi Yamashita, Kinya Otsu, Ichiro Manabe, Ryozo Nagai, Issei Komuro
Diterbitkan 2019-06-01Dapatkan teks lengkap
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